Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> NUF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163347833:163347833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747173543
CDS Mutation	c.1019C>T
AA Mutation	p.Ser340Leu(p.S340L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163347926:163347926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775293541
CDS Mutation	c.1112G>A
AA Mutation	p.Arg371His(p.R371H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163327536:163327536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172G>A
AA Mutation	p.Gly58Arg(p.G58R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163348992:163348992(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1172T>C
AA Mutation	p.Val391Ala(p.V391A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000271452
Start	163348945:163348945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1125G>T
AA Mutation	p.Glu375Asp(p.E375D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163336768:163336768(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355C>T
AA Mutation	p.Arg119Trp(p.R119W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163338056:163338056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61747498
CDS Mutation	c.472G>A
AA Mutation	p.Ala158Thr(p.A158T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163355407:163355407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1333T>A
AA Mutation	p.Tyr445Asn(p.Y445N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163340421:163340421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536480913
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163343824:163343824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761A>G
AA Mutation	p.Tyr254Cys(p.Y254C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163336769:163336769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781627921
CDS Mutation	c.356G>A
AA Mutation	p.Arg119Gln(p.R119Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271452
Start	163326081:163326081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567182286
CDS Mutation	c.30T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271452
Start	163328272:163328272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.243C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271452
Start	163336755:163336755(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.345delA
AA Mutation	p.Lys115AsnfsTer7(p.K115Nfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000271452
Start	163349015:163349016(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1201dupA
AA Mutation	p.Ile401AsnfsTer2(p.I401Nfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> NUF2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000271452
Start	163349080:163349080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1260G>T
AA Mutation	p.Gln420His(p.Q420H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163326150:163326150(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99G>T
AA Mutation	p.Lys33Asn(p.K33N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163343777:163343777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714G>T
AA Mutation	p.Glu238Asp(p.E238D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163345711:163345711(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.841G>T
AA Mutation	p.Asp281Tyr(p.D281Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271452
Start	163347833:163347833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747173543
CDS Mutation	c.1019C>T
AA Mutation	p.Ser340Leu(p.S340L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript